OT non salt/c: I need support - MS like or MS (Was MS or Lyme)

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This forum has helped me greatly. I write to all who are people of faith  and/or people with experience. I don't see a difference between MS like symptoms and MS. I've come to understand  there are virus' that affect the body and the affects manifest differently, I think, because of genetic differences and whatever else might be going on.

What's the difference between MS and MS like symptoms? I'm thinking

there are none. Even if I entertained MS, which I won't, I would still

do what I'm doing: salt/c and soon CS-silver 100, B-12 shots, soon vit d3 and mag oli.I've read about LDN and salt/c and CS all helping both. What do people do here neuro symptoms affecting gait, coordination, vison, e.g MS like symptoms?

I recently saw a neuro who is a MS specialist. I was referred to her by my Lyme neurologist. Anticipating her diagnosis I was prepared. She tells me it's classic MS. She doesn't recognize late stage/chronic Lyme. Although I have have lesions on my brain (2006 MRI) and cervical spine, I learned some of the lesions on my brain are gone (2009 mri)  and there are no enhanced (active) lesions.

Thanks,BE wellstacy